Literature DB >> 1840101

Recent biochemical and genetic advances in our understanding of Batten's disease (ceroid-lipofuscinosis).

N A Hall1, B D Lake, A D Patrick.   

Abstract

Protein is the major component of the intra-lysosomal storage material which characteristically accumulates in Batten's disease. In the late-infantile, juvenile and adult forms of the disease, and in a form affecting sheep, this protein is principally composed of a single polypeptide, subunit c of mitochondrial ATP synthase. Subunit c is not stored in the infantile form of Batten's disease, supporting recent genetic data which suggest this is a distinct disease. Nor is subunit c found in storage material within other lysosomal storage diseases or in lipofuscin of old age. Subunit c storage, therefore, is specific for the later-onset forms of Batten's disease and indeed may be central to their aetiology.

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Year:  1991        PMID: 1840101     DOI: 10.1159/000112183

Source DB:  PubMed          Journal:  Dev Neurosci        ISSN: 0378-5866            Impact factor:   2.984


  2 in total

1.  Juvenile neuronal ceroid-lipofuscinosis: characterization of the dyslipoproteinaemia and demonstration of membrane phospholipid and phospholipid-dependent signal transduction abnormalities in cultured skin fibroblasts.

Authors:  M J Bennett; S F Poirier; L Chern; A R Gayton; G P Hosking; N A Le; S Majumdar; H M Korchak
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

Review 2.  Making yeast tremble: yeast models as tools to study neurodegenerative disorders.

Authors:  Michael Y Sherman; Paul J Muchowski
Journal:  Neuromolecular Med       Date:  2003       Impact factor: 3.843

  2 in total

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